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Asthma clinical trials

View clinical trials related to Asthma.

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NCT ID: NCT00649025 Completed - Asthma Clinical Trials

A Study Comparing the Safety and Efficacy of Fluticasone and Formoterol Combination (FlutiForm™) With Fluticasone or Flovent to Treat Moderate to Severe Asthma in Adolescents and Adults

Start date: March 2008
Phase: Phase 3
Study type: Interventional

The medications being used in this study are individually approved by the Food and Drug Administration (FDA). The medication under investigation is a combination of two medications in one inhaler. The purpose of this study is to determine how well your asthma is controlled when taking one of the three treatment.

NCT ID: NCT00646789 Completed - Asthma Clinical Trials

A Study to Evaluate the Safety, Tolerability and Plasma Concentration Profiles of MK0633 in Asthmatic Children Aged 12 to Less Than 16 Years (0633-019)

Start date: May 2008
Phase: Phase 1
Study type: Interventional

To evaluate the safety, tolerability and pharmacokinetics (PK) of MK0633 in adolescent mild-to-moderate asthma patients to permit further clinical investigation.

NCT ID: NCT00646620 Completed - Asthma Clinical Trials

Symbicort Onset of Action 1

Start date: April 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the early onset of effect of Symbicort compared to Advair Diskus and Ventolin in adults with asthma

NCT ID: NCT00646594 Completed - Asthma Clinical Trials

Atlantis Symbicort

Start date: November 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether Symbicort compared with Advair, will be more effective in controlling asthma in adults and adolescents.

NCT ID: NCT00646529 Completed - Asthma Clinical Trials

Long-Term Safety of Symbicort in Asthmatic Children - SAPLING

Start date: July 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the safety of Symbicort compared to Pulmicort in asthmatic children aged 6 to 11 years

NCT ID: NCT00646321 Completed - Asthma Clinical Trials

Efficacy of Symbicort pMDI Administered Once Daily in Children and Adolescents During 12 Weeks - SPROUT

Start date: April 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare Symbicort with budesonide alone for the treatment of asthma in children aged 6 to 15 years

NCT ID: NCT00646009 Completed - Asthma Clinical Trials

Symbicort Onset of Action 2

Start date: March 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the early onset of effect of Symbicort compared to Advair Diskus and Ventolin in adults with asthma

NCT ID: NCT00644514 Terminated - Healthy Clinical Trials

Genetics of Asthma - Bronchoscopy Studies

Start date: September 2007
Phase: Phase 1
Study type: Interventional

The purpose of this study is to identify the mediators and genes in airway epithelial and BAL cells that are differentially regulated following inhalation of endotoxin lipopolysaccharide (LPS) among study participants with allergic asthma and normal phenotypes. This approach is designed to identify novel genes associated with both asthma pathogenesis and asthma susceptibility. LPS, or endotoxin, a cell wall component of gram-negative bacteria, is ubiquitous in the environment, and is thought to influence both susceptibility and severity of asthma. 240 subjects (healthy adult men and women (age >18-40) with and without atopy and asthma) will complete the screening evaluations in order to establish 3 study groups of 60 subjects each. Each qualified subject will undergo an inhaled LPS endotoxin challenge followed by bronchoscopy after 24 hours, which will consist of a bronchoalveolar lavage (BAL) and endobronchial brush biopsies. BAL involves squirting a small amount of sterile salt water into one of the airways then gently taking it back out through the bronchoscope. The brush sample involves gently moving a small brush back and forth in an airway to collect cell samples. Samples of whole blood will also be obtained at various time points. RNA will be isolated from these cell populations in order to assess differential gene expression expression using microarrays.

NCT ID: NCT00644462 Not yet recruiting - Asthma, Bronchial Clinical Trials

Wheeze Detection in Adults During Dynamic Bronchial Situations Measured by PulmoTrack® 2010 With WIM-PC™ Technologies Recording

Start date: June 2009
Phase: N/A
Study type: Observational

The PulmoTrack® 2010 with WIM-PC™ Technologies device, indicated for acoustic pulmonary function measurement that quantifies the presence of wheezing. This study was designed in order to evaluate the efficacy and safety of using the WIM-PC™ device for wheeze detection during dynamic bronchial situations in asthmatic adult.

NCT ID: NCT00643578 Completed - Asthma Clinical Trials

Dose-response of Inhaled Formoterol Using Methacholine Challenge as a Bioassay

Start date: March 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to find out whether a difference between two doses of formoterol can be detected by methacholine challenge.